Classifications

• • G—PHYSICS
  • G02—OPTICS
  • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
  • G02B5/00—Optical elements other than lenses
  • G02B5/30—Polarising elements
  • G02B5/3083—Birefringent or phase retarding elements
• • G—PHYSICS
  • G02—OPTICS
  • G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
  • G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
  • G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
  • G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells
  • G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
  • G02F1/1333—Constructional arrangements; Manufacturing methods
  • G02F1/1335—Structural association of cells with optical devices, e.g. polarisers or reflectors
  • G02F1/13363—Birefringent elements, e.g. for optical compensation
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
  • C08J5/18—Manufacture of films or sheets
• • G—PHYSICS
  • G02—OPTICS
  • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
  • G02B5/00—Optical elements other than lenses
  • G02B5/30—Polarising elements
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
  • C09K2323/00—Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition

Definitions

• the present invention relates to a retardation film. More specifically, the present invention relates to a retardation film using an amorphous polyolefin copolymer comprising an ethylene unit and a norbornene unit.
• Amorphous polyolefin is a polyolefin that has an alicyclic structure to make it heat resistant and amorphous, and is characterized by excellent dimensional stability due to its high transparency and low water absorption. Furthermore, since it does not contain an aromatic component, it has a feature that the photoelastic constant is extremely low. With the increase in the size of liquid crystal display devices for televisions and the like, its excellent physical properties are gradually attracting attention.
• Such amorphous polyolefins can be broadly classified into two in terms of structure. One is obtained by ring-opening polymerization of cyclic olefin, and then hydrogenating the double bond of the main chain that is produced.
• Product names ZEONEX (registered trademark), ZEONOR (registered trademark) manufactured by Nippon Zeon Co., Ltd. (Trademark), JSR Co., Ltd., and other products such as ARTON (registered trademark) are already on the market.
• the other is a product obtained by copolymerizing cyclic olefin with ethylene and vinyl, and is commercially available under the trade name APEL (registered trademark) manufactured by Mitsui Chemicals, Inc., and manufactured by TI CONA.
• TOPA s registered trademark
• the former type of ring-opening polymerization and hydrogenation has so far been studied as a retardation film, such as retardation characteristics, production methods, and incorporation into liquid crystal display devices
• Japanese Patent Laid-Open No. Hei 4- Japanese Patent No. 3 2 7 3 0 4 6, Japanese Patent Laid-Open No. 6-5 9 1 2 1, Japanese Patent Laid-Open No. 8-4 3 8 1 2, Japanese Patent No. 3 4 7 No. 0 5 6 7 and Japanese Patent No. 2 0 0 3-3 0 6 5 5 7).
• the latter copolymer of cyclic olefin and ethylene can be produced in one stage of polymerization compared to the former, and although it is advantageous in terms of economy, its properties as a retardation film are almost known so far. There wasn't.
• the vinyl-type copolymer resins such as thermoplastic polyolefin and cyclic polyolefin are also listed as desirable resins. However, there are few examples that have been specifically examined.
• amorphous polyolefin generally has a very low photoelastic constant, and has the essential property that birefringence is less likely to develop than aromatic polymers such as polycarbonate and polysulfone. Therefore, in the case of a resin in which birefringence hardly develops even when the film is stretched, the film thickness must be considerably increased to obtain a retardation film having a desired retardation value, and thinness and lightness are required. It is no longer suitable as a component of the liquid crystal display device.
• a Ziegler-Natsuya catalyst represented by a combination of a nonadium compound and an organic aluminum compound is used. Or metal complex such as titanium and zirconium and MAO (methylaluminoxane)
• a method of polymerizing using a meta-orthene catalyst comprising a cocatalyst such as the above is practical.
• the Ziegler-Natta catalyst is difficult to control the composition and steric structure because of its polymerization mechanism, and is therefore known to give a tactic polymer with poor stereoregularity by random copolymerization.
• the meta-octacene catalyst has a uniform active site and can be controlled in various ways. For example, it has been confirmed that the stereoregularity of the resulting copolymer varies depending on the difference of the ligand of meta-octene (see Macrol. Rap id Commun. 2 Q_, 279 (1999)). . In addition, it has been reported that the difference affects the mechanical properties and melt properties of the copolymer (Japanese Patent Publication No. 8-50 7800, Japanese Patent Publication No. 8-507801 and Japanese Patent Publication No. 7-2953). The difference in optical properties has not been studied so far. Disclosure of the invention
• the object of the present invention has been made in view of the above-mentioned situation, and in the latter type of amorphous polyolefin, which is advantageous in terms of economy, that is, in the copolymer of cyclic olefin and ethylene. It is to provide a retardation film suitable for. Another object of the present invention is to provide an unoriented film for the retardation film.
• Still another object of the present invention is to provide a liquid crystal display device provided with the retardation film.
• the norbornene unit contains two chain sites, the stereoregularity of the two chain sites is meso-type and racemo-type, and the ratio of meso-type two-chain sites norracemo-type two-chain sites is 4 or more, and
• the above objects and advantages of the present invention are secondly, This is achieved by an unoriented film for producing the retardation film of the present invention.
• the above object and advantage of the present invention are as follows.
• FIG. 1 is a 13 C-NMR spectrum chart of an ethylene-norbornene copolymer containing 44 mol% of the norbornene component obtained in Example 1.
• FIG. 2 is a chart of a 13 C-NMR spectrum of grade 6013 of trade name TOP AS, manufactured by TI CON A, used in Examples 2 to 5.
• FIG. 3 is a 13 C-NMR spectrum chart of an ethylene-norbornene copolymer containing 42 mol% of the norbornene component obtained in Comparative Example 1.
• FIG. 4 is a chart of 13 C-NMR spectrum of Darred 5013, trade name TOP AS manufactured by TI CONA, used in Comparative Example 2. Preferred embodiments of the invention
• the amorphous polyolefin used in the present invention is a copolymer obtained by vinyl polymerization of ethylene and norbornene.
• a copolymer consisting of an ethylene repeating unit (A) and a norbornene repeating unit (B) represented by the following formula: Coalescence is mentioned.
• R G1 and R Q2 are each independently a hydrogen atom or an alkyl group having 1 to 10 carbon atoms.
• norbornene compounds giving the norbornene repeating unit (B) include bicyclo [2.2.1] hept-2-ene, 6-methylbicyclo [2.2.1] hept-2-ene, 5, 6 _Dimethylbicyclo [2.2.1] hepto-2-ene, 6-ethylbicyclo [2.2.1] hept-2-ene and 6-butylbicyclo [2.2.1] hept-2-ene Can be mentioned. Of these, bicyclo [2.2.1] hept-2-ene, in which R 0 1 and R Q 2 are both hydrogen atoms, is preferred.
• the amorphous polyolefin may contain a small amount of repeating units composed of other copolymerizable vinyl monomers as long as the object of the present invention is not impaired.
• other vinyl monomers include cyclic olefins represented by the following formula (C):
• n is 0 or 1
• m is 0 or a positive integer
• p is 0 or 1
• 1 ⁇ ⁇ 1 ⁇ 2 () is the same or different
• R 17 and R 18 , or R 19 and R 2 Q form an alkylidene group.
• R 17 or R 18 and R 19 or R 2Q may form a ring, and the ring may have a double bond.
• Replacement paper examples include Q! —Olefins such as octadecene, cycloolefin, cyclobutene, cyclopentene, cyclohexene, 3-methylcyclohexene, and cycloolefins such as cyclooctene.
• monoolefin having 3 to 18 carbon atoms can be used as a molecular weight regulator in copolymerization, and among these, 1-hexene is preferably used.
• Such other vinyl monomers may be used alone or in combination of two or more, and the repeating unit thereof is preferably 10 mol% or less, more preferably 5 mol% or less.
• an ethylene-norbornene copolymer depends on a polymerization method, a catalyst to be used, a composition, and the like, but in any case, some chain sites of norbornene units exist.
• NN diamond stereoregularity at the two-chain site (hereinafter referred to as NN diamond) of the norpolymerene unit of vinyl polymerization type
• meso form of formula (D) and racemo form of (E) meso form of formula (D) and racemo form of (E)
• the copolymer of the present invention the following formulas (D) and (E)
• the ratio of the meso type 2 linked site represented by (Rasemo type) to the racemo type 2 linked site is 4 or more in the ratio of meso type 2 linked site / rasemo type 2 linked site.
• the ratio is 6 or more.
• the upper limit of the ratio is not particularly limited, and the higher the ratio, the better the expression of birefringence and the more preferable.
• the existence of the NN dyad stereoisomer here The ratio is determined by 13 C-NMR based on the report analyzing the stereoregularity of ethylene-norbornene copolymer (see Macro 1. Rap id Commu n. 20, 279 (1999) mentioned above). It is possible.
• the ratio of the meso-type 2-linked site norracemo-type 2-linked site is [28.3 ppm peak area of 13 C-NMR spectrum] / [ It was calculated as equivalent to the ratio of the peak area of 29.7 ppm in the 13 C-NMR spectrum.
• this ratio becomes smaller than 4, that is, the proportion of the racemo type increases, the copolymer becomes less birefringent.
• the thickness is increased, the stretching ratio is increased, and the stretching temperature is lowered. In some cases, a desired phase difference value can be obtained by such means, but it is not preferable from the viewpoints of thinning and productivity.
• the analysis by 13 C-NMR can also determine the abundance ratio (molar fraction) of NN dyads relative to the total amount of norbornene unit components, that is, how much the norbornene unit forms a chain structure. It is in the range of 1 to 0.6.
• the glass transition temperature (Tg) of such a copolymer is in the range of 100 to 1 80. When Tg is lower than 100, the heat stability is poor.
• Tg is higher than 180 ° C, the toughness of the film tends to decrease, and the melt viscosity of the copolymer becomes too high, making it difficult to melt and form the film.
• Such a composition can be determined by 13 C-NMR measurement.
• the molecular weight of the ethylene-norbornene copolymer used in the present invention is as follows: a reduced viscosity of 7?
• Sp / c measured in a cyclohexane solution at a temperature of 30 and a concentration of 1.2 gZd L. More preferably, it is within the range of 0 d LZ g and 0.3 to 3 d LZg. If the reduced viscosity is 7? S pZ c is less than 0.1, the film becomes fragile, which is not preferable. If it is greater than 10, for example, when melt film formation is performed, the melt viscosity becomes too high and it becomes difficult to melt the film. .
• one type of copolymer may be used as it is, or two or more types of copolymers having different compositions and molecular weights may be blended and used.
• the above preferred composition and molecular weight indicate the entire blend.
• the method for producing the ethylene-nornorpinene copolymer used in the present invention is not particularly limited as long as the glass transition temperature and the NN diode stereoregularity satisfy the above ranges. Specifically, a method of copolymerizing ethylene and norbornene using a meta-octacene catalyst can be preferably mentioned.
• the metamouth used in this case is the following formula (F)
• M is a metal selected from the group consisting of titanium, zirconium or hafnium
• R 24 and R 25 are the same or different and are a hydrogen atom, a halogen atom, or a C 1-12 saturated.
• an unsaturated hydrocarbon group, an alkoxy group having 1 to 12 carbon atoms, or an aryloxy group having 6 to 12 carbon atoms, and R 2 2 and R 23 is the same or different, and is a monocyclic or polycyclic hydrocarbon group capable of forming a Sant Germanti structure with the central metal M
• 21 is a bridge connecting 22 shaku and! 2 3 groups
• R 26 to R 29 are the same or different and are a hydrogen atom, a halogen atom, a saturated or unsaturated hydrocarbon group having 1 to 12 carbon atoms, an alkoxy group having 1 to 12 carbon atoms, or carbon. It is an aryloxy group of the number 6 to 12, or R 26 and R 27 or R 28 and R 29 may form a ring.
• R 22 and R 23 are preferably a cyclopentaenyl group, an indenyl group, an alkyl or aryl thereof, and the central metal M is most preferably zirconium in terms of catalytic activity.
• R 24 and R 25 may be the same or different, but are preferably an alkyl group having 1 to 6 carbon atoms or a halogen atom, particularly a chlorine atom.
• R 26 to R 29 are preferably a hydrogen atom, an alkyl group having 1 to 6 carbon atoms or a phenyl group, and R 21 is methyl.
• Preferred examples include lower alkylene groups such as ethylene groups, ethylene groups, propylene groups, alkylidene groups such as isopropylidene, substituted alkylene groups such as diphenylmethylene, silylene groups, or substituted silylene groups such as dimethylsilylene and diphenylsilylene. it can.
• preferred metacenes include isopropylidene (cyclopentenyl) (1 indenyl) zirconium dichloride, isopropylidene [(3-methyl) cyclopentyl] (1-indenyl) zirconium dichloride, dimethylsilylene (Cyclopentaphenenyl) (1 Indenyl) Zirconium Dichloride, Dimethylsilylene-bis (1-Indenyl) Zirconium Dichloride, Diphenylsilylene-bis (1-Indenyl) Zirconium Dichloride, Ethylene Monobis (1-Indenyl) Zirconium Examples thereof include dichloride, isopropylidene bis (11 indenyl) zirconium dichloride, and the like.
• metallocene promoter a known catalyst such as methylaluminoxane, which is an organoaluminum compound, or a combination of an ionic boron compound and an alkylaluminum compound can be used.
• the desired copolymer can be polymerized by a known polymerization method using a hydrocarbon solvent such as toluene, xylene, cyclohexane or the like.
• a hydrocarbon solvent such as toluene, xylene, cyclohexane or the like.
• the retardation film of the present invention can be produced by obtaining a normally unstretched, unoriented film for forming such a copolymer and subjecting it to stretching, and then stretching the film.
• the unstretched film can be formed by a known method such as a solution casting method, a melt extrusion method, a hot pressing method, or a calendar method.
• the melt extrusion method is preferable from the viewpoint of productivity and economy, and from the viewpoint of solvent-free environment.
• Melt press In the dispensing method, a method of extruding the resin using a T die and feeding it to a cooling roll is preferably used.
• the temperature at the time of extrusion is determined in consideration of the fluidity, thermal stability, etc. of the copolymer, but it is preferably performed in the range of 220 ° C. to 300 ° C. for the copolymer of the present invention.
• the melt viscosity of the copolymer becomes too high, and if it exceeds 300, the copolymer may be degraded and degraded, and the transparency and homogeneity of the film may be impaired due to gelation. More preferably, it is in the range of 220 ° C to 280.
• a hydrocarbon solvent such as toluene, xylene, cyclohexane, or decalin is preferably used. In the production of an unstretched film by these methods, it is preferable to reduce the film thickness unevenness as much as possible.
• the film thickness unevenness is preferably ⁇ 8% or less, more preferably ⁇ 5% or less with respect to the film thickness.
• the thickness in the unstretched film stage is determined in consideration of the desired retardation value and film thickness in the stretched retardation film, but is preferably in the range of 30 to 400 / xm, more preferably It is in the range of 40 to 300 mm, particularly preferably in the range of 40 to 250 m.
• the retardation film of the present invention can be obtained by stretching and orienting the unstretched film thus obtained.
• the stretching method is not particularly limited, and a known method such as longitudinal uniaxial stretching that stretches between rolls, lateral uniaxial stretching using a tenter, or simultaneous biaxial stretching that combines them, or sequential biaxial stretching can be used.
• An axially oriented film can be obtained.
• the stretching temperature is in the range of (Tg—20 ° C) to (Tg + 30 ° C) with respect to the glass transition temperature (Tg) of the ethylene-norbornene copolymer, preferably (Tg_10 ° C) to (Tg + 20 ° C).
• the draw ratio is determined by the target retardation value, but it is 1.05 to 4 times, and more preferably 1.:! ⁇ 3 times.
• liquid crystal display devices such as TN type, STN type, TFT type, transmissive type, reflective type, and transflective type, and also TN mode, vertical alignment (VA) mode, OC
• TN mode vertical alignment
• VA vertical alignment
• OC Various modes such as B mode and IPS mode have been developed.
• the properties of the retardation film required vary depending on the type of liquid crystal used and the mode, but the ethylene-norbornene copolymer of the present invention has a good birefringence, so it is a thin film. It is possible to provide retardation films having various characteristics.
• an in-plane retardation R (550) at a wavelength of 550 nm is in the range of the following formula (1):
• phase difference R is defined by the following formula (5), and is a characteristic representing the phase delay of light transmitted in the direction perpendicular to the film.
• R (550) is more preferably from 100 to 600 nm, and further preferably from 120 to 600 nm. Further, the thickness is more preferably 20 to 120, and further preferably 20 to 80 m.
• Such a retardation film can be prepared by uniaxial stretching or biaxial stretching, and can be suitably used for a 1 ′′ 4 ⁇ plate, a 1/2 ⁇ plate, a ⁇ plate, and the like.
• an in-plane retardation R (550) at a wavelength of 550 nm and a retardation K (550) in the film thickness direction are expressed by the following formulas (2) and (3):
• K (550) is a retardation value in the film thickness direction at a wavelength of 550 nm, and is defined by the following formula (4).
• nx and ny are the x and y axes in the film plane! ! Is the refractive index in the thickness direction perpendicular to the axis and axis, and d is the thickness of the film.
• phase difference R is more preferably 10 to 80 nm, still more preferably 30 to 80 nm.
• (55 0) is more preferably from 80 to 250 nm.
• the thickness is more preferably 30 to 100 m, still more preferably 30 to 85 m.
• Such a retardation film can be prepared by biaxial stretching, has birefringence in the film thickness direction of the film, and is particularly suitably used for optical compensation in a vertical alignment (VA) mode.
• VA vertical alignment
• the optical compensation configuration in the vertical alignment mode for large liquid crystal display devices such as televisions consists of a two-sheet configuration in which the optical compensation film is sandwiched on both sides of the liquid crystal cell and a single-sheet configuration that is used only on one side of the liquid crystal cell. is there.
• the retardation film of the present invention used in a two-sheet configuration includes 30 nm ⁇ R (550) ⁇ 80 nm, 80 nm ⁇ K (55
• the retardation film of the present invention is excellent in birefringence, it can be suitably used as a single-layer retardation film requiring a high K value. In the liquid crystal display element of the vertical alignment mode incorporating these retardation films, the contrast is good when viewed from an oblique direction as well as from the front, and a wide viewing angle can be obtained.
• the retardation film of the present invention has the following (i), (i)
• the norbornene unit contains two linked sites, the stereoregularity of the two linked sites is meso-type and racemo-type, and the ratio of meso-type 2-linked site Z racemo-type 2-linked site is 4 or more.
• phase difference R (550) in the film surface due to light having a wavelength of 550 nm satisfies the following formula (1 1 1) 120 nm and R (550) ⁇ 600 ('1 1 1) A retardation film with a film thickness in the range of 20-80 zm.
• the norbornene unit contains two linked sites, the stereoregularity of the two linked sites is meso-type and racemo-type, and the ratio of meso-type 2-linked site / rasemo-type 2-linked site is 4 or more.
• phase difference R (550) in the film surface due to light with a wavelength of 550 nm is expressed by the following equations (2-1) and (3-1)
• the norbornene unit contains two linked sites, the stereoregularity of the two linked sites is meso-type and racemo-type, and the ratio of meso-type 2-linked site racemo-type 2-linked site is 4 or more, And
• phase difference R (550) in the film surface due to light with a wavelength of 550 nm is expressed by the following equations (2_ 1) and (3-2) 3 0 nm ⁇ R (5 5 0) ⁇ 80 nm-- ⁇ (2-1)
• a retardation film is used by being laminated between a liquid crystal cell and a polarizing film.
• TAC triacetyl cellulose
• PVA polyvinyl alcohol
• the retardation film of the present invention can be used by either method.
• the retardation film of the present invention can be produced by either a continuous method or a batch method, but it is preferable to continuously stretch the film from an industrial viewpoint.
• the film to be conveyed can be wound around a winding core, and a retardation film can be obtained in a rolled form.
• both those in which the slow axis is oriented in the width direction of the film and those in which the slow axis is oriented in the traveling direction of the film can be produced.
• a biaxially oriented film can be preferably mentioned.
• a longitudinally uniaxially oriented film obtained by longitudinally uniaxially stretching an unstretched film, laterally stretched after longitudinal stretching, or longitudinally stretched after lateral stretching is finally obtained. Examples thereof include a biaxially oriented film in which the slow axis is longitudinally oriented.
• the biaxially oriented film has a slow axis in the width direction of the film. What can be bonded with a polarizing plate roll and a so-called roll tO roll is preferable from the viewpoint of productivity.
• Example The present invention will be described more specifically with reference to the following examples. However, the present invention is not limited to these examples.
• Toluene (solvent) and norbornene were all distilled and purified and dried thoroughly.
• ethylene di-bis (1 indenyl) zirconium dichloride purchased from A 1 d r i c h was used as it was.
• Isopropylidene (9-fluorenyl) (cyclopentenyl) Zirconium dichloride was synthesized according to the literature [J. A. Ewe neta 1, J. Am. Chem. S oc., 110, 6255-6266 (1988)]. .
• polymethylaluminoxane (PM AO) was purchased from Tosoh Axo Co., Ltd., prepared in a 2M concentration toluene solution and used.
• Triisobutylaluminum (i Bu) 3A 1] was purchased from Kanto Chemical Co., Inc. with a 1M n-hexane solution and used as it was.
• Glass transition temperature (Tg) A 2920 type DSC made by TA In ns tr ume nts was used, and the heating rate was 20 and measured in minutes.
• Photoelastic constant of film Measured with a spectroscopic ellipsometer Ml 50 manufactured by JASCO Corporation. It was calculated from the change in retardation value when stress was applied to the film at a measurement wavelength of 550 nm.
• the reaction mixture was discharged into a large amount of methanol acidified with hydrochloric acid to precipitate a precipitate, which was separated by filtration, repeatedly washed with acetone, methanol and water, and dried to obtain 20.3 g of a resin.
• the Tg was 120 ° C. 13 C—NMR Figure 1 shows the spectrum obtained from the measurement. From Fig. 1, it was found that the racemo type of NN diads at 29.7 ppm was hardly observed and only the real meso type at 28.3 ppm.
• the abundance ratio (molar fraction) of NN diad to the total amount of norbornene component was 0.21.
• a 2 Owt% solution was prepared, and a film with a film thickness of 58 m was obtained by the solution casting method.
• the film had a total light transmittance of 91.1% and a haze of 1.1%.
• Tg was 107 and became lower due to the effect of residual solvent. Also it was determined light ⁇ number constant of the film - 6. was 3 X 10- 12 P a- 1.
• the film was stretched using a batch-type biaxial stretching apparatus in which the film end was fixed with a chuck. The horizontal direction was free and longitudinal uniaxial stretching was performed under the conditions shown in Table 1, and the film thickness and phase difference R (550) of the center of the film after stretching were measured. The results are shown in Table 1.
• TOPAS (trade name) manufactured by TI CONA is a cycloolefin copolymer obtained by copolymerizing ethylene and norbornene with a meta-cene catalyst. Its grade 601
• Figure 2 shows the spectrum.
• the molecular weight was 0.80 dLZg in reduced viscosity? S pZc.
• the pellet is melt-extruded from a T-die with a width of 15 cm using a twin-screw melt extruder (TEX30 S S-42 BW-3 V manufactured by Nippon Steel Co., Ltd.) and continuously wound with a cooling roller.
• the film forming conditions were as follows: cylinder temperature 260t: T die temperature 270 ° C, cooling roller temperature 145 ° C, film forming speed 1 mZ. Film was transparent, homogeneous and excellent in surface quality. It was. Except for the 2.5 cm width at both ends of the film, the film thickness averaged 120 m. Tg was 138 ° C, total light transmittance was 91.5%, and haze was 0.3%. Also was determined photoelastic constant of the full Ilm - 6. was 1 X 10_ 12 P a- 1. The film was subjected to longitudinal uniaxial stretching in the same manner as in Example 1. The stretching conditions and results are shown in Table 1.
• Example 2 In film formation by melt extrusion performed in Example 2, the slit width of the T die was changed to obtain a molten film having an average film thickness of 190 m. Tg was also 13 8: the total light transmittance was 91.4% and haze was 0.4%. This film was successively biaxially stretched 1.5 times in length and 2.0 times in width by the batch type biaxial stretching apparatus used in Example 2. The film thickness R (550) and K (550) at the center of the film after stretching were measured. The results are shown in Table 1.
• a melt film was created. Film formation was performed in the same manner as in Example 2 except that the cooling roller temperature was lowered to 130. The film had a total light transmittance of 90.8% and a haze of 0.8%, and was highly transparent and homogeneous. Except for the 2.5 cm width at both ends of the film, the film thickness averaged 180 m. Also was one 6. 0X 10- 12 P a one 1 was determined photoelastic constant of the film. The Tg was one at 125 ° C, indicating that both resins were compatible.
• the molecular weight was 0.88 dLZg with a reduced viscosity of 77 s pZc.
• the resin was dissolved in cyclohexane to prepare a 2 Owt% solution, and a film having a thickness of 65 m was obtained by a solution casting method.
• the film had a total light transmittance of 91.6% and a haze of 0.5%. Tg decreased to 105 ° C due to the influence of residual solvent. Also was one 9. 2 X 10- 12 P a- 1 was determined light ⁇ constant of the film. The unstretched film was longitudinally uniaxially stretched under the conditions shown in Table 1. The results are shown in Table 1. The phase difference value was extremely low.
• TOPAS (trade name) grade 5013 (Tg 140 ° C) 13 C—NM R measurement was performed.
• Figure 4 shows the spectrum.
• the molecular weight was 0.66 dLZg with a reduced viscosity of 7? S pZc.
• the pellet was extruded under the same conditions as in Example 2 to obtain a molten film.
• the film was excellent in transparency and homogeneity, and had good surface properties.
• the film thickness averaged 82 / zm except for the 2.5 cm width at both ends of the film.
• Tg was 137 ° C
• total light transmittance was 90.7%
• haze was 0.5%.
• the photoelastic constant of the film - 9. A 3X 10- 12 P a- 1.
• the unstretched film was subjected to longitudinal uniaxial stretching in the same manner as in Example 1. The stretching conditions and results are shown in Table 1. The phase difference value was extremely low.
• Example 7 Roll uniaxially oriented roll film
• Example 8 Roll uniaxially oriented roll film
• the unstretched roll film obtained in Example 7 was composed of three zones, a preheating zone, a stretching zone, and a fixing / cooling zone, and was subjected to transverse stretching using a tenter transverse stretching machine having a total length of 15 m.
• the film was stretched 2.7 times at a speed of 5 m / min and a temperature of 142 ° C., and a laterally uniaxially oriented film was wound up.
• Table 2 shows the film characteristics. Slow in the width direction of the film A retardation film having a phase axis in the vicinity of ⁇ / 4 was obtained.
• Example 9 Rolled film for V ⁇ mode using two sheets of vertical to horizontal biaxial orientation
• the same conditions were applied except that the film forming speed of the melt extrusion performed in Example 7 was changed to 2 mZ.
• a roll film having a width of 300 mm and an average thickness of 15 3 was obtained.
• the film was excellent in transparency, surface properties and homogeneity.
• This film was passed through the longitudinal stretching machine used in Example 7, and stretched 1.5 times at a rate of 3.3 mZ on the inlet side. Subsequently, the film was passed through the transverse stretching machine used in Example 8 and stretched 2.0 times at a speed of 5 mZ to obtain a biaxially oriented film.
• Table 2 shows the stretching conditions and film characteristics.
• a film suitable for a large VA mode retardation film having a two-layer structure having a slow axis in the width direction of the film was obtained.
• Example 10 0 roll film for VA mode using one sheet of vertical to horizontal biaxial orientation
• the film was formed under the same conditions except that the film forming speed of the melt extrusion performed in Example 7 was changed to 1.4 mZ.
• the film was excellent in transparency, surface properties and homogeneity.
• This film was passed through the longitudinal stretching machine used in Example 7 and stretched 2.0 times at an entry side speed of 2.5 mZ. Subsequently, the film was passed through the transverse stretching machine used in Example 8 and stretched 2.5 times at a speed of 5 mZ to obtain a biaxially oriented film.
• Table 2 shows the stretching conditions and film characteristics.
• a film suitable for a single-layer large VA mode retardation film having a slow axis in the width direction of the film was obtained.
• Example 1 1 (VA mode liquid crystal display device)
• Example 10 The film prepared in Example 10 was attached to a polyvinyl alcohol polarizing plate so that the slow axis of the film and the transmission axis of the polarizing plate were aligned.
• This laminate is bonded to one side of the TFT-type liquid crystal cell for VA mode so that the retardation film side is the liquid crystal cell side, and the other side of the liquid crystal cell is pasted so that the polarizing plate is crossed Nicol to create a display device. did.
• Such a display device was not colored even when viewed from the oblique direction as compared with the case without the retardation film, and the contrast was good.
• Table 2 Table 2
• aThe film travel direction is 0 °.
• a thin retardation film can be obtained by using the above-mentioned copolymer having a low photoelastic constant and good birefringence among ethylene-cyclic olefin copolymers. Obtainable.
• the retardation film has high moisture resistance and good dimensional stability.For example, it is incorporated into a liquid crystal display device and is effectively used to improve the display quality of liquid crystals, such as viewing angle improvement, contrast improvement, and color compensation. be able to.

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